HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88719671A>C , CM000678.2:g.88719671A>C | GRCh38 |
NC_000016.9:g.88786079A>C , CM000678.1:g.88786079A>C | GRCh37 |
NC_000016.8:g.87313580A>C | NCBI36 |
NG_042229.1:g.70550T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301015.14:c.6374T>G MANE Select | ENSP00000301015.9:p.Val2125Gly | |
ENST00000466823.3:c.400T>G | ||
ENST00000301015.13:c.6374T>G | ENSP00000301015.9:p.Val2125Gly | |
ENST00000419505.5:c.140T>G | ENSP00000406358.1:p.Val47Gly | |
ENST00000466823.2:c.400T>G | ||
ENST00000495568.7:n.615T>G | ||
ENST00000497793.2:n.529T>G | ||
NM_001142864.2:c.6374T>G | NP_001136336.2:p.Val2125Gly | |
NM_001142864.3:c.6374T>G | NP_001136336.2:p.Val2125Gly | |
NM_001142864.4:c.6374T>G MANE Select | NP_001136336.2:p.Val2125Gly |